A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17063988



Internal ID21502268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24253074..24253074hg38UCSC Ensembl
chr1:24579564..24579564hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg383366
hg193366
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5619828
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17063988
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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